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Differential Diagnosis For Presentation/Progressive CNS degeneration Acidosis Myopathy Liver Child


List of current finding(s):

Metabolic, Storage Disorders
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Infantile mitochondrial myopathy/Cox defect
Hereditary, Familial, Genetic Disorders
Hereditary mitochondrial disorder
0-11 years old, Acidoses, acidosis, Acidosis (disorder), Child, Child (person), Child Youth, Childhood age person, Childhood age person (person), Children, Children (0-21), disease (or disorder) muscle, Disorder muscle, Disorder of muscle, Disorder of muscle unspec, Disorder of muscle unspecified, Disorder of muscle unspecified (disorder), Disorder of skeletal AND/OR smooth muscle (disorder), Disorders of muscles, MUSCLE DIS, MUSCLE DISEASE, Muscle disease or syndrome, Muscle Disorder, Muscle Disorders, MUSCULAR DIS, Muscular Disease, Muscular Diseases, muscular disorder, Muscular Disorders, Myopathic Condition, Myopathic Conditions, Myopathic disease, Myopathic disease or syndrome, Myopathic Diseases and Syndromes, Myopathic syndrome, MYOPATHIES, Myopathy, Myopathy (disorder), Myopathy unspecified, Presentation, Progressive cerebellar degeneration, Unspecified disorder of muscle
External Links Related to Presentation/Progressive CNS degeneration Acidosis Myopathy Liver Child
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)